RESUMEN
The rational choice of an electron acceptor was proved to be an effective strategy for the development of novel electron transfer (ET) photochromic iodides, but the types and amounts of reported electron acceptors are relatively limited so far, especially for monocyclic aromatic molecules. Herein, using monocyclic pyridinium derivatives (N-protonation-4-carboxypyridinium/N-protonation-4-carbamoylpyridinium/1-methyl-4-(carbomethoxy)pyridinium) as structural directing agents and electron acceptors, five new electron donor-acceptor-based halo-argentate/cuprate hybrids or iodide salts have been synthesized, including [HINA][Ag4I5] (1), [HINAM]I (2), [HINAM]I·0.5(I2) (3), [MCMP][Ag2Br3] (4) and [MCMP][Cu2I3] (5). Noteworthily, compounds 1-3 exhibit interesting photochromic behaviours, while compounds 4 and 5 are non-photochromic. Finally, the possible chromic mechanisms and influencing factors for the title compounds were also discussed.
RESUMEN
Three isostructural halozincates, [HNH][ZnX4]·H2O (HNH2+ = protonated nicotinohydrazide, X = I (1), Br (2), Cl (3)), have been synthesized and exhibit halogen-dependent photoinduced electron transfer and chromic properties. Due to the different electron-donating nature of halogen atoms, only iodozincate hybrid 1 can easily undergo photoinduced electron transfer and eye-detectable photochromic behavior, revealing a unique matching rule between a moderate electron acceptor and halozincates.
RESUMEN
By using 1-methyl-4-(carbomethoxy)pyridinium (MCMP+) as counterions, two iodoargentate hybrids, 1D [MCMP][AgI2] (1) and 3D [MCMP][Ag3I4] (2) have been synthesized and they exhibit rare electron transfer photochromism with a fast response rate, a wide response range and a long-lived charge-separated state in iodometallate systems. Noteworthily, the marked differences in the structure and photochromic performance of 1 and 2 are largely ascribed to the different aggregating behavior of electron-deficient MCMP+ counterions (C-HO hydrogen bonded trimer in 1 and π-π/C-Hπ chain in 2).
RESUMEN
By employing in situ methylnicotinohydrazide dication (MNH(2+)) as an electron acceptor, we have constructed an iodocuprate(I) hybrid {[MNH][Cu2I3]2}n (1), which exhibits charge transfer (CT) thermochromism due to the intense absorption of CT and electron transfer (ET) photochromism with high photocoloration contrast and fast response to UV irradiation due to the synergetic effect of valence change of copper ions.
